V. Kimonis

Genotype–phenotype studies of VCP‐associated inclusion body myopathy with Paget disease of bone and/or frontotemporal dementia

J. Platt, M. Pasquali, K. Osann, 2013, Clinical genetics.

A multicenter study of maternal and neonatal outcomes in individuals with Prader-Willi syndrome

D. J. Driscoll, V. Kimonis, M. Butler, 2018 .

Novel VCP mutations in inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia

D. Drachman, A. Kaminska, C. Weihl, 2007, Clinical genetics.